Thin Pt films on the polar SrTiO3(111) surface:: an experimental and theoretical study

被引:56
作者
Asthagiri, A
Niederberger, C
Francis, AJ
Porter, LM
Salvador, PA
Sholl, DS [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Mat Sci & Engn, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
titanium; alkaline earth metals; platinum; epitaxy; density functional calculations; metallic films; x-ray scattering; diffraction; and reflection;
D O I
10.1016/S0039-6028(03)00609-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have examined the growth of thin Pt films on the polar SrTiO3(111) surface using both experimental and theoretical methods. Pt films were grown on both as-received and treated substrates using electron-beam evaporation, and then were characterized with X-ray and low-energy electron diffraction and atomic force microscopy. The nature of the substrate surface strongly influences the crystallinity and microstructure of the Pt films. We find that for well-treated, crystalline SrTiO3(111) substrates we obtain crystalline Pt(111) films. In addition, the first few layers strongly replicate the surface structure of the substrate. XRD results demonstrate that even the best films exhibit two distinct inplane domains separated by 60degrees, equivalent to the existence of inversion domains. Density functional theory (DFT) calculations were performed for 1-4 monolayers of Pt on both terminations of SrTiO3(1 11). These calculations find that two energetically equivalent stacking sequences are possible for the second monolayer of Pt, corresponding to the observed 60degrees domains. We propose that these stacking faults are the source of the observed domains in crystalline Pt(111) films grown on polar SrTiO3(111) surfaces. Finally, the DFT calculations corroborate the observation that the structures and growth modes of the first few monolayers are coupled strongly to the substrate, yet the films quickly relax to bulk-like Pt arrangements and homoepitaxial growth modes. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:134 / 152
页数:19
相关论文
共 56 条
[1]   First principles study of Pt adhesion and growth on SrO- and TiO2-terminated SrTiO3(100) [J].
Asthagiri, A ;
Sholl, DS .
JOURNAL OF CHEMICAL PHYSICS, 2002, 116 (22) :9914-9925
[2]  
ASTHAGIRI A, UNPUB
[3]   Adhesive energy and charge transfer for MgO/Cu heterophase interfaces [J].
Benedek, R ;
Minkoff, M ;
Yang, LH .
PHYSICAL REVIEW B, 1996, 54 (11) :7697-7700
[4]   Role of surface vacancies and water products in metal nucleation: Pt/MgO(100) [J].
Bogicevic, A ;
Jennison, DR .
SURFACE SCIENCE, 1999, 437 (1-2) :L741-L747
[5]   Variations in the nature of metal adsorption on ultrathin Al2O3 films [J].
Bogicevic, A ;
Jennison, DR .
PHYSICAL REVIEW LETTERS, 1999, 82 (20) :4050-4053
[6]   Low-symmetry diffusion barriers in homoepitaxial growth of Al(111) [J].
Bogicevic, A ;
Stromquist, J ;
Lundqvist, BI .
PHYSICAL REVIEW LETTERS, 1998, 81 (03) :637-640
[7]   THE HOMOEPITAXIAL GROWTH OF PT ON PT(111) STUDIED WITH STM [J].
BOTT, M ;
MICHELY, T ;
COMSA, G .
SURFACE SCIENCE, 1992, 272 (1-3) :161-166
[8]   Electronic structure of the polar ZnO{0001}-surfaces [J].
Carlsson, JM .
COMPUTATIONAL MATERIALS SCIENCE, 2001, 22 (1-2) :24-31
[9]   GROUND-STATE OF THE ELECTRON-GAS BY A STOCHASTIC METHOD [J].
CEPERLEY, DM ;
ALDER, BJ .
PHYSICAL REVIEW LETTERS, 1980, 45 (07) :566-569
[10]   Adhesion of ultrathin ZrO2(111) films on Ni(111) from first principles [J].
Christensen, A ;
Carter, EA .
JOURNAL OF CHEMICAL PHYSICS, 2001, 114 (13) :5816-5831